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P Deloukas

Showing results (21-30 of 51) with videos related to

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Journal of Medical Genetics|April 11, 2009
A genome-wide association study identifies a novel locus on chromosome 18q12.2 influencing white cell telomere lengthM Mangino, J B Richards, N Soranzo, et al.
The Pharmacogenomics Journal|May 11, 2005
Common VKORC1 and GGCX polymorphisms associated with warfarin doseM Wadelius, L Y Chen, K Downes, et al.
Arteriosclerosis, Thrombosis, and Vascular Biology|January 24, 2009
Large scale association analysis of novel genetic loci for coronary artery disease, N J Samani, P Deloukas, et al.
Diabetes, Obesity & Metabolism|January 16, 2009
Overview of the MHC fine mapping dataW M Brown, J Pierce, J E Hilner, et al.
Nature|March 10, 2001
Comparison of human genetic and sequence-based physical mapsA Yu, C Zhao, Y Fan, et al.
Genomics|June 6, 1998
A detailed physical and transcriptional map of the region of chromosome 20 that is deleted in myeloproliferative disorders and refinement of the common deleted regionA J Bench, M A Aldred, S J Humphray, et al.
Journal of Medical Genetics|June 11, 2009
A genome-wide association study suggests that a locus within the ataxin 2 binding protein 1 gene is associated with hand osteoarthritis: the Treat-OA consortiumG Zhai, J B J van Meurs, G Livshits, et al.
Oncogene|August 22, 2000
Chromosome 20 deletions in myeloid malignancies: reduction of the common deleted region, generation of a PAC/BAC contig and identification of candidate genes. UK Cancer Cytogenetics Group (UKCCG)A J Bench, E P Nacheva, T L Hood, et al.
Diabetologia|September 6, 2008
Genetic association analyses of non-synonymous single nucleotide polymorphisms in diabetic nephropathyD A Savage, C C Patterson, P Deloukas, et al.
Gene|January 30, 2002
Identification and characterization of a novel human brain-specific gene, homologous to S. scrofa tmp83.5, in the chromosome 10q24 critical region for temporal lobe epilepsy and spastic paraplegiaC Nobile, B Hinzmann, P Scannapieco, et al.
Pageof 6

Showing results (21-30 of 51) with videos related to

Sort By:
Pageof 6
Journal of Medical Genetics|April 11, 2009
A genome-wide association study identifies a novel locus on chromosome 18q12.2 influencing white cell telomere lengthM Mangino, J B Richards, N Soranzo, et al.
The Pharmacogenomics Journal|May 11, 2005
Common VKORC1 and GGCX polymorphisms associated with warfarin doseM Wadelius, L Y Chen, K Downes, et al.
Arteriosclerosis, Thrombosis, and Vascular Biology|January 24, 2009
Large scale association analysis of novel genetic loci for coronary artery disease, N J Samani, P Deloukas, et al.
Diabetes, Obesity & Metabolism|January 16, 2009
Overview of the MHC fine mapping dataW M Brown, J Pierce, J E Hilner, et al.
Nature|March 10, 2001
Comparison of human genetic and sequence-based physical mapsA Yu, C Zhao, Y Fan, et al.
Genomics|June 6, 1998
A detailed physical and transcriptional map of the region of chromosome 20 that is deleted in myeloproliferative disorders and refinement of the common deleted regionA J Bench, M A Aldred, S J Humphray, et al.
Journal of Medical Genetics|June 11, 2009
A genome-wide association study suggests that a locus within the ataxin 2 binding protein 1 gene is associated with hand osteoarthritis: the Treat-OA consortiumG Zhai, J B J van Meurs, G Livshits, et al.
Oncogene|August 22, 2000
Chromosome 20 deletions in myeloid malignancies: reduction of the common deleted region, generation of a PAC/BAC contig and identification of candidate genes. UK Cancer Cytogenetics Group (UKCCG)A J Bench, E P Nacheva, T L Hood, et al.
Diabetologia|September 6, 2008
Genetic association analyses of non-synonymous single nucleotide polymorphisms in diabetic nephropathyD A Savage, C C Patterson, P Deloukas, et al.
Gene|January 30, 2002
Identification and characterization of a novel human brain-specific gene, homologous to S. scrofa tmp83.5, in the chromosome 10q24 critical region for temporal lobe epilepsy and spastic paraplegiaC Nobile, B Hinzmann, P Scannapieco, et al.
Pageof 6